lipid metabolism in pregnancy and its consequences in the fetus and newborn
TRANSCRIPT
Received July 26, 2002; Accepted July 26, 2002.
Author to whom all correspondence and reprint requests should be addressed:
Dr. Emilio Herrera, Universidad San Pablo-CEU, Ctra. Boadilla del Monte
km 5,300, E-28668 Boadilla del Monte, Madrid, Spain. E-mail: eherrera@
ceu.es
Lipid Metabolism in Pregnancyand its Consequences in the Fetus and Newborn
Emilio Herrera
Facultad de Ciencias Experimentales y de la Salud, Universidad San Pablo-CEU, Madrid, Spain
Endocrine, vol. 19, no. 1, 43–55, October 2002 0969–711X/02/19:43–55/$20.00 © 2002 by Humana Press Inc. All rights of any nature whatsoever reserved.
43
During early pregnancy there is an increase in bodyfat accumulation, associated with both hyperphagiaand increased lipogenesis. During late pregnancy thereis an accelerated breakdown of fat depots, which playsa key role in fetal development. Besides using placen-tal transferred fatty acids, the fetus benefits from twoother products: glycerol and ketone bodies. Althoughglycerol crosses the placenta in small proportions, it isa preferential substrate for maternal gluconeogenesis,and maternal glucose is quantitatively the main sub-strate crossing the placenta. Enhanced ketogenesisunder fasting conditions and the easy transfer of ketonesto the fetus allow maternal ketone bodies to reach thefetus, where they can be used as fuels for oxidativemetabolism as well as lipogenic substrates. Althoughmaternal cholesterol is an important source of choles-terol for the fetus during early gestation, its impor-tance becomes minimal during late pregnancy, owingto the high capacity of fetal tissues to synthesize cho-lesterol. Maternal hypertriglyceridemia is a character-istic feature during pregnancy and corresponds to anaccumulation of triglycerides not only in very low-density lipoprotein but also in low- and high-densitylipoprotein. Although triglycerides do not cross theplacental barrier, the presence of lipoprotein recep-tors in the placenta, together with lipoprotein lipase,phospholipase A2, and intracellular lipase activities,allows the release to the fetus of polyunsaturated fattyacids transported as triglycerides in maternal plasmalipoproteins. Normal fetal development needs theavailability of both essential fatty acids and long chainpolyunsaturated fatty acids, and the nutritional statusof the mother during gestation has been related tofetal growth. However, excessive intake of certain longchain fatty acids may cause both declines in arachi-donic acid and enhanced lipid peroxidation, reducingantioxidant capacity.
Key Words: Lipid metabolism; pregnancy; placenta;fatty acids; cholesterol; triglycerides.
Introduction
Fetal development is sustained by the metabolites cross-
ing the placenta at the expense of those present in maternal
circulation. Glucose is quantitatively the most important
nutrient crossing the placenta, followed by amino acids
(1–5), and the development of the fetus directly depends on
their continuous availability. However, although the pla-
cental transfer of lipid components is very limited (6), they
also play a major role in fetal development. Changes in
the availability of lipid components, like those produced
by changes in dietary fatty acids, are known to have impli-
cations in fetal and postnatal development (7). In addi-
tion, adaptations of maternal lipid metabolism taking place
throughout gestation also have major consequences for fetal
growth. It is known that deviations in maternal hyperlipi-
demia, such as those caused by hypercholesterolemia, even
when temporary and limited to pregnancy, trigger patho-
genic events in the fetal aorta and may lead to atheroscle-
rosis later in life (8–10). Two consistent manifestations of
altered maternal lipid metabolism normally occurring dur-
ing gestation are the accumulation of lipids in maternal tis-
sues (11,12) and the development of maternal hyperlipidemia
(13,14). Conditions known to alter any of these manifesta-
tions by impairing maternal fat depot accumulation, such
as hypothyroidism or overt diabetes during the first half of
gestation, greatly affect fetal growth at late gestation, even
if they are compensated for by appropriate hormonal treat-
ment during the second half of gestation (15,16). These
findings therefore emphasize the important role of mater-
nal lipid metabolism on fetal growth and late pregnancy out-
come, despite the difficulties of lipids crossing the placenta.
This article reviews the changes that occur in maternal
lipid metabolism during gestation and how they contribute
to fetal and postnatal development.
Adipose Tissue Metabolism: Lipolytic Activity
An accelerated breakdown of fat depots occurs in both
women and rats during the last third of gestation (17–21),
and higher activity and mRNA expression of the key enzyme
for adipose tissue lipolysis, hormone-sensitive lipase, in late
pregnant rats have been reported (22). As will be discussed,
despite the enhanced release of lipolytic products, nonester-
ified fatty acids (NEFA) and glycerol into maternal circu-
lation, their placental transfer is quantitatively low (6). The
Herrera (2590).p65 12/9/2002, 8:35 AM43
Lipid Metabolism in Pregnancy / Herrera44 Endocrine
main destiny of these products is the liver (23), where, after
the conversion of NEFA into acyl-CoA and glycerol into
glycerol-3-phosphate, they are reesterified for the synthesis
of triglycerides (Fig. 1). These are incorporated into nascent
very low-density lipoprotein (VLDL) particles, which are
then released into the circulation, where they are converted
into mature VLDLs. Since insulin may inhibit VLDL secre-
tion (24), a maternal insulin-resistant condition may contrib-
ute to the increased VLDL production. However, augmented
estrogen concentration at late pregnancy seems to be the
major activator of VLDL liver production (14).
Under fasting conditions during late pregnancy, mater-
nal adipose tissue lipolytic activity becomes highly enhanced
(20,21,25,26). A heightened catecholamine excretion (27,
28) secondary to maternal hypoglycemia even under mild
dietary deprivation, together with the increased amount of
gestational hormones released by the placenta and ovary,
as well as the insulin-resistant condition, seems to be respon-
sible for higher lipolytic activity of maternal adipose tissue.
Maternal plasma concentration of glycerol and NEFA
increase during late gestation (21,26,29) as a consequence
of the enhanced adipose tissue lipolytic activity. Besides the
use of those lipolytic products in the synthesis of triglycer-
ides, glycerol may be used for glucose synthesis and NEFA
for �-oxidation to acetyl-CoA and ketone body synthesis.
These metabolic pathways become enhanced under fasting
conditions at late pregnancy, when the use of glycerol for
gluconeogenesis is even higher than other more classic glu-
coneogenetic substrates, such as alanine and pyruvate (30,
31). Under this condition of food deprivation, ketogenesis
is also greatly heightened in maternal liver (32,33).
Increased gluconeogenesis from glycerol and ketogen-
esis from NEFA may benefit the fetus, which at late gesta-
tion is at its maximum accretion rate and its requirements
for substrates and metabolic fuels are greatly augmented.
The preferential use of glycerol for gluconeogenesis and
the efficient placental transfer of the newly formed glucose
may be of major importance to the fetus under these fasting
conditions (Fig. 2), in which the availability of other essen-
tial substrates such as amino acids is reduced (30,34). Placen-
tal transfer of ketone bodies is highly efficient (35), reaching
fetal plasma at the same level as in maternal circulation (29).
Ketone bodies may be used by the fetus as fuels (36) and as
substrates for brain lipid synthesis (37).
Accumulation of Body Fat
Accumulation of fat is one of the most common charac-
teristics of pregnancy, occurring in both women (11,12,38)
and experimental animals (39–42), and accounts for most
of the conceptus-free increase in maternal body weight dur-
ing gestation (12,39,43). The increase in maternal fat depots
occurs during the first two-thirds of gestation, whereas it
declines or even stops during the last third (11,39,44,45),
the latter corresponding to the phase of most accelerated lipo-
lytic activity of adipose tissue.
Fig. 1. Schematic representation of utilization by the liver of adipose tissue lipolytic products, NEFA and glycerol, as substrates for
triglyceride synthesis and VLDL production for their catabolism by extrahepatic tissues. LPL = Lipoprotein lipase.
Herrera (2590).p65 12/9/2002, 8:35 AM44
Lipid Metabolism in Pregnancy / HerreraVol. 19, No. 1 45
Accumulation of body fat during early pregnancy has been
associated with both hyperphagia and increased lipogene-
sis. Hyperphagia is present in both pregnant women (46,47)
and rats (41,48), and increases as gestational time advances.
This progressive increase in the availability of exogenous
substrates actively contributes to maternal accumulation of
fat depots. As recently reviewed, the total energy cost of fat
deposition in women from poor countries is lower than in
those from well-nourished populations (49), and in the rat
it is not found under food-restricted conditions (41,42,48).
Fatty acid and glyceride glycerol synthesis from glu-
cose by rat periuterine adipose tissue in situ progressively
increases until d 20 of gestation to sharply decline on d 21
(50,51) (Fig. 3). Enhanced fatty acid synthesis was also
found in pregnant rats when studied in vivo (52), and this
increased lipid synthesis seems to actively contribute to the
fat accumulation occurring during gestation.
A proportional increase in adipose tissue lipoprotein lipase
(LPL) activity could also contribute to the fat accumulation
found during early pregnancy. This enzyme is normally bound
Fig. 2. Schematic representation of role of adipose tissue triglyceride stores as source of NEFA and glycerol for liver ketogenesis and
gluconeogenesis during late pregnancy in fasting condition, to sustain availability of substrates for fetal and maternal tissues.
Fig. 3. Glucose utilization for fatty acid and glyceride glycerol synthesis by periuterine adipose tissue in situ during gestation in rat.
Methodologic details are as described in ref. 51. *Statistical comparisons vs virgin rats (0 d: *p < 0.05, **p < 0.01, ***p < 0.001).
Herrera (2590).p65 12/9/2002, 8:35 AM45
Lipid Metabolism in Pregnancy / Herrera46 Endocrine
in its active form to the capillary endothelium of extrahep-
atic tissues (53) and hydrolyzes triglycerides circulating in
plasma in the form of triglyceride-rich lipoproteins, chylo-
microns, and VLDLs (Fig. 1), which are respectively con-
verted into remnant particles and intermediate-density lipo-
proteins. The hydrolytic products, NEFA and glycerol, are
partially taken up by the subjacent tissue (54), and, there-
fore, LPL controls the fat uptake in adipose tissue. Although
a few reports have shown that at d 12 of gestation in preg-
nant rats there is an increase in the LPL activity of adipose
tissue (34,55), the change is small and not always repro-
duced (22). No significant change has been found in the post-
heparin LPL activity in pregnant women at midgestation
(13). Thus, enhanced LPL activity of adipose tissue does not
seem to contribute substantially to the accumulation of body
fat taking place during the first part of gestation.
However, during late pregnancy, adipose tissue LPL con-
sistently decreases in the rat (44,56–58), and postheparin
LPL also decreases in women at the third trimester of preg-
nancy (13,59). These findings indicate that fat uptake by adi-
pose tissue decreases during late pregnancy, which together
with the enhanced lipolytic activity mentioned earlier, result
in a net accelerated breakdown of fat depots. Thus, the ana-
bolic condition of adipose tissue present during early preg-
nancy switches to a net catabolic condition during the last
trimester of pregnancy, coinciding with the phase of maxi-
mal fetal growth. These changes contribute to the develop-
ment of maternal hyperlipidemia, which besides other lipids,
includes increments in plasma levels of NEFA (60), spar-
ing glucose, which is essential not only to certain maternal
tissues, such as brain, but also to sustain fetal development.
Enhanced maternal insulin levels and changes in insulin
sensitivity taking place throughout pregnancy may be directly
or indirectly responsible for the early anabolism and late
catabolism present in maternal adipose tissue in pregnancy.
During early pregnancy, heightened activity of pancreatic
�-cells is developed, as shown by the augmented insulino-
tropic effect of glucose seen in both women and rats (61–
63). At this stage, insulin sensitivity is either unchanged or
even augmented (64–66). Since both glycerolgenesis and
lipogenesis from glucose are pathways sensitive to insulin,
maternal hyperinsulinemia whenever the mother eats must
contribute to her active deposition of fat depots. The situ-
ation changes drastically during the last third of gestation,
when, despite maternal hyperinsulinemia, a major insulin-
resistant condition develops (66–70). The reversion of insu-
lin resistance in the late pregnant rat (71), as well as studies
in isolated adipocytes from pregnant women (18), has shown
that insulin resistance is responsible for both enhanced adi-
pose tissue lipolytic activity and decreased LPL activity of
adipose tissue (72).
The transition from an anabolic to a catabolic condition
in maternal adipose tissue metabolism coincides with the
maximal fetal growth phase (44,66), i.e., when the mother
needs to progressively increase the supply to the fetus. As
discussed next, this situation causes the development of mater-
nal hyperlipidemia, which spares glucose and other essential
metabolites, such as amino acids, for the fetus, and there-
fore is of major importance not only to maternal metabolic
economy but to fetal development.
Hyperlipidemia
Maternal hypertriglyceridemia is also a characteristic
feature during late pregnancy, whereas rises in phospho-
lipids and cholesterol are smaller (14). This change corre-
sponds not only to an increment in VLDLs but also to an
enrichment of triglycerides in other lipoprotein fractions
that normally do not transport them, such as low-density
lipoproteins (LDLs) and high-density lipoproteins (HDLs)
(13). Even within the HDL subfractions, there is a specific
increment in the proportion of triglycerides in the HDL2b
subfraction at the expense of the HDL2a
or HDL3, which
are rich in cholesterol (13). The greatest increase in plasma
triglycerides corresponds to the VLDL triglycerides (13,
73), synthesized in the liver. The main factors inducing this
increase in plasma VLDL triglycerides during gestation
are their enhanced production by the liver (74,75) and their
decreased removal from the circulation as a consequence
of reduced LPL activity of adipose tissue (13,22).
An increase in cholesteryl ester transfer protein activity
taking place at midgestation (13,76), together with the abun-
dance of VLDL triglycerides, seems to contribute to the accu-
mulation of triglycerides in the other lipoproteins, LDL
and HDL (13,73), which under nonpregnant conditions are
normally poor in this lipid moiety. Another factor contrib-
uting to this same effect is the decrease in the hepatic lipase
activity, which also occurs during late pregnancy (13). The
decrease in this enzyme activity decreases the conversion
of buoyant HDL2 triglyceride-rich particles into small HDL
3
triglyceride-poor particles, allowing a proportional accu-
mulation of the former (13). These interactions taking place
in lipoprotein metabolism during late pregnancy are sche-
matically summarized in Fig. 4.
Both the insulin-resistant condition and the increase in
plasma estrogen levels occurring during late pregnancy are
the main hormonal factors responsible for these metabolic
changes addressing to the development of maternal hyper-
triglyceridemia. The insulin-resistant condition constantly
present during late gestation is known to contribute to both
enhanced lipolytic activity of adipose tissue, which, as dis-
cussed, augments the arrival of glycerol and NEFA to the
liver and their subsequent conversion into triglycerides, which
are released back into the circulation in the form of VLDL
(71), and the decreased LPL activity (72). The progressive
increase in plasma estrogen levels during gestation (77,78)
also actively contributes to maternal hypertriglyceridemia;
it has been shown to enhance liver production of VLDL (79,
80) and decrease the expression and activity of hepatic lipase
in liver (81,82).
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Lipid Metabolism in Pregnancy / HerreraVol. 19, No. 1 47
Role of Maternal Hypertriglyceridemia
as a Source of Fatty Acids for the Fetus
Although triglycerides do not directly cross the placental
barrier (6), essential fatty acids (EFA) derived from mater-
nal diet, which are transported as triglycerides in triglycer-
ide-rich lipoproteins in maternal plasma (7), must become
available to the fetus. Placental trophoblast cells have been
shown to express both very low-density/apo E receptor as
well as LDL receptor–related proteins (83–88). In addition,
they also express LPL activity (89–91) as well as phospholip-
ase A2 (92,93) and intracellular lipase activities (94–96).
Maternal triglycerides in plasma lipoproteins are there-
fore hydrolyzed and taken up by the placenta, where they
are reesterified to provide a reservoir of fatty acids (97).
After the intracellular hydrolysis of glycerides releases fatty
acids diffusely to fetal plasma, they bind to a specific onco-
fetal protein, the �-fetoprotein (98,99). Fatty acids are then
rapidly transported to fetal liver, where they are reesterified
and released back into circulation in the form of triglycerides.
Because the amount of polyunsaturated fatty acids present
in plasma in the form of NEFA represents a minor propor-
tion as compared to those carried in the form of lipoproteins
(7) (Fig. 5), the mechanism described indicates that maternal
hyperlipoproteinemia plays a key role in the availability of
EFA to the fetus. In fact, a linear correlation has been found
between maternal and fetal plasma triglycerides in the rat
(7,100), and a direct relationship between maternal triglyc-
erides and newborn weight has been found in humans (101–
103). Furthermore, a reduction in maternal hypertriglyceri-
demia, such as that caused by treatments with hypolipidemic
drugs, has negative effects in fetal development (104,105).
Transfer of Lipid Metabolites to the Fetus
Nonesterified Fatty Acids
The net flux of fatty acids crossing the placenta differs
among species. In species with a placenta having both mater-
nal and fetal layers, such as sheep, pig, and cat, the maternal
fetal fatty acid transfer is small (106–109). In species in which
the placenta is formed by layers of fetal origin, such as rab-
bit (110), guinea pig (111), primate (112), and rat (113,114),
the amount of fatty acids crossing the placenta exceeds even
that needed to fulfill lipid storage requirements (115). In
humans, although in a smaller proportion than lipoprotein tri-
glycerides (Fig. 5), maternal plasma NEFA are an important
source of polyunsaturated fatty acids for the fetus (116,117).
The plasma membrane fatty acid–binding protein present
in human placental membranes (118,119) is responsible
for the preferential uptake of long chain polyunsaturated
fatty acids (LCPUFA). Besides the preference for human
placental transfer for certain fatty acids—docosahexaenoic
(DHA) > �-linolenic > linoleic > oleic > arachidonic acid
(AA) (120)—the uptake of arachidonic acid by syncytio-
trophoblast membranes has been shown to occur via an
active process, highly dependent on ATP and sodium (121).
A selective cellular metabolism of certain fatty acids may
Fig. 4. Schematic representation of lipoprotein interactions during third trimester of pregnancy, causing an increase in triglyceride (TG)
content of main plasma lipoprotein fractions. IDL, intermediate-density lipoproteins; CETP, cholesterol ester transfer protein; CE, cho-
lesterol esters; HL, hepatic lipase. See text for additional explanations.
Herrera (2590).p65 12/9/2002, 8:35 AM47
Lipid Metabolism in Pregnancy / Herrera48 Endocrine
also contribute to the placental transfer process, as would
the conversion of a certain proportion of arachidonic acid to
prostaglandins (117), the incorporation of some fatty acids
into phospholipids (122), the oxidation of placental fatty
acids (123), and the synthesis of fatty acid (124).
The combination of all these processes determines the
actual rate of placental fatty acid transfer and its selectivity,
resulting in the proportional enrichment of certain LCPUFA,
such as AA and DHA in fetal as compared with maternal com-
partments (125).
We have recently found that the concentration of PUFA
in plasma lipoproteins in pregnant women during the third
trimester of pregnancy is much greater than that in NEFA
(7) (Fig. 5), and previous evidence indicates that circulating
triglycerides contribute to plasma fetal fatty acids in the rat
(126), rabbit (90), guinea pig (127), and human (128). There-
fore, although lipoprotein triglycerides do not directly cross
the placental barrier, as already mentioned, the placenta has
mechanisms to release fatty acids circulating in maternal
plasma lipoproteins into the fetus.
Glycerol
Plasma glycerol levels are consistently elevated during
late pregnancy (22,129). Their values are higher in the mother
than in the fetus, although with some interspecies differ-
ences. The maternal/fetal glycerol gradient is greater in those
species with an epitheliochorial placenta (130), as is the case
of ruminants, than in those with a hemochorial placenta (131,
132). Although having low molecular weight and uncharged
structure, glycerol would be adequate for easy placental trans-
fer. However, the actual amount of glycerol that crosses the
placenta is much lower than other metabolites with similar
molecular characteristics such as glucose or L-alanine (2,
66,133). Different from these two metabolites, transfer of
placental glycerol is carried out by means of a simple dif-
fusion mechanism (2), and the reason for its small placental
transfer may reside in both its low concentration and its
short half-life in maternal plasma, which limits its avail-
ability. This hypothesis is supported by the fact that hepa-
tectomy and nephrectomy in pregnant rats causes a smaller
increase in plasma glycerol than in nonpregnant rats. This
difference is not a consequence of reduced lipolytic activ-
ity in the pregnant rat because plasma NEFA increases even
more than in nonpregnant animals. Fetal plasma glycerol
appears higher in hepatectomized and nephrectomized rats
than in controls, indicating a higher transfer to the fetus in
the former (23).
Thus, transfer of placental glycerol seems to be limited by
the effective and rapid utilization of this substrate through
other pathways, such as gluconeogenesis (30,134) and glyc-
eride glycerol synthesis (132), and therefore its low plasma
concentration and very active kinetics impede the forma-
tion of the adequate gradient to create the appropriate driv-
ing force for its placental transfer.
Ketone Bodies
In the third trimester of pregnancy, under fed conditions,
plasma ketone body levels remain low, but they greatly
increase compared to nonpregnant conditions under fasting
(32,33,135) or in diabetes (73,136,137), as a consequence
of enhanced adipose tissue lipolysis, which accelerates the
delivery of NEFA to the liver and enhances ketogenesis.
As mentioned, besides being used by maternal tissues as
alternative substrates for glucose, ketone bodies can easily
cross the placenta and be used as fuels and lipogenic sub-
strates by the fetus. Maternal hyperketonemia in the poorly
controlled diabetic patient and secondary transfer of exces-
sive arrival of ketone bodies to the fetus seem to be respon-
sible for major damage there (138), increasing stillbirth
rate, incidence of malformations, and impaired neurophysi-
ologic development (139–141).
The transfer of ketone bodies across the placenta occurs
either by simple diffusion or by a low-specificity carrier-
mediated process (35,130), whose efficiency varies among
species, being much lower in the ruminant than in the non-
ruminants. This causes major differences in the maternofetal
Fig. 5. Proportional distribution of PUFA in plasma NEFA and
lipoprotein fractions in women during the third trimester of preg-
nancy and at postpartum (2–6 mo). Lipoproteins were isolated by
sequential ultracentrifugation and PUFA are quantified as previ-
ously described (73,206). EC, esterified cholesterol; PHL, phos-
pholipids; TG, triglycerides.
Herrera (2590).p65 12/9/2002, 8:35 AM48
Lipid Metabolism in Pregnancy / HerreraVol. 19, No. 1 49
gradient for ketone bodies, which is above 10 in ruminants
(138,142), around 2 in humans (143) and 1 in the rat (144,
145), indicating that the amount of ketone bodies crossing
the placenta is much lower in ruminant than in nonruminant
species. A similar relationship may be proposed for the con-
tribution of ketone bodies to fetal oxidative metabolism,
which is only 2 to 3% in the case of sheep (146). In the rat,
however, 3-hydroxybutyrate may replace glucose deficit in
the placenta, as well as in fetal brain and liver during fasting
hypoglycemia (36), suggesting a much greater contribution
of ketone bodies to the fetal oxidative metabolism.
The activity of ketone body metabolizing enzymes is pres-
ent in fetal tissues (brain, liver, and kidney) (36,37,139,
147) and can be increased by conditions of maternal keto-
nemia such as starvation, during late pregancy (148) or high-
fat feeding (149). These changes may represent an important
adaptation to guarantee brain development under these con-
ditions of limited availability of other substrates and may
represent a special preservation of fetal brain compared with
other fetal organs.
Therefore, in nonruminant species there is evidence for
an effective placental ketone body transfer and its efficient
use by the fetus as substrates for both oxidation and lipo-
genesis. Although these processes are concentration depen-
dent, their quantitative contribution to fetal metabolism is
only relevant under conditions of maternal hyperketonemia
(e.g., starvation, high-fat intake, and diabetes) (36).
Cholesterol
Cholesterol plays a key role in embryonic and fetal devel-
opment. It is an essential component of cell membranes,
where it contributes to membrane fluidity and passive per-
meability by interacting with phospholipids and sphingo-
lipids (150). Cholesterol is the precursor of bile acids and
steroids, and in the fetus at late pregnancy there is an intense
synthesis of glucocorticoids in the adrenals. Cholesterol is
also required for cell proliferation (151,152) and plays impor-
tant roles in cell differentiation and cell-to-cell communica-
tion (153). In addition, cholesterol and its oxidative deriva-
tives, oxysterols, are key regulators of different metabolic
processes (154–156). The demands for cholesterol in the
embryo and the fetus are therefore relatively high. The fetus
may obtain cholesterol from endogenous synthesis as well
as from the yolk sac and the placenta.
Placental transfer of maternal cholesterol has been shown
to be effective in different species, such as rat (157), guinea
pig (158), and rhesus monkey (159), although the estimated
contributions of maternal cholesterol to the fetus were quite
variable, mainly owing to methodologic reasons. Choleste-
rol synthesis in fetal tissues, and especially in fetal brain, is
highly active in different species, even higher than in mater-
nal tissues when expressed per mass unit (160–164). These
findings are consistent with the high level of mRNA expres-
sion of different enzymes involved in cholesterol synthesis
(165) and the high activity of 3-hydroxy-3-methyl glutaryl
coenzyme A reductase, the rate-limiting enzyme of choles-
terol synthesis, in fetal tissues (166,167).
In the rat, it has been shown that the fetus receives little
or no cholesterol from the mother, satisfying its need for
cholesterol through endogenous synthesis (163,164). Feed-
ing pregnant rats with cholesterol, which resulted in increased
plasma cholesterol concentration and reduced maternal chol-
esterol synthesis, did not affect any of these parameters in the
fetus (160,161,168,169) or fetal development (170). All of
these findings led to the conclusion that in the rat, during
late gestation, fetal cholesterol originates mainly from endog-
enous de novo synthesis rather than from placental trans-
fer. However, during the early stages of gestation, maternal
cholesterol contributes substantially to fetal cholesterol. This
is why treatments with an inhibitor of �6-reductase, AY
9944, result in fetal teratogenesis, but simultaneous admin-
istration of oral cholesterol during early pregnancy completely
prevents this effect (171–173). These findings indicate that
during early pregnancy in the rat, maternal cholesterol reaches
the fetus and plays an important physiologic role.
In humans, it has been found that umbilical venous
levels of HDL-, LDL-, and total-cholesterol concentrations
were higher than in umbilical arterial plasma at term, indi-
cating the delivery of cholesterol from the placenta to the
fetus, but the contribution of this cholesterol to the fetal
plasma cholesterol pool was very small (174). Comparison
of mater-nal lipoprotein-cholesterol levels and those in
mixed umbil-ical cord blood cholesterol gave either a posi-
tive correlation (175,176) or no correlation between these
values (174,177–179). Gestational age could influence these
comparisons, since plasma fetal cholesterol levels have been
found higher in 5- than in 7-mo-old fetuses (8). In fetuses
younger than 6 mo, plasma cholesterol levels are signifi-
cantly correlated to the maternal ones (8), suggesting that
maternal cholesterol actively contributes to fetal cholesterol
in early gestation.
The presence of several lipoprotein receptors in the pla-
centa (84,180) and, to a lesser extent, in the yolk sac (181)
allow these tissues to take up cholesterol from maternal
lipoproteins, although the contribution of this process to
the export of cholesterol to the fetus remains to be clarified.
Role of Dietary Fatty Acids in the Offspring
Normal fetal development needs not only the EFA but
also their LCPUFA derivatives to support the synthesis of
structural lipids (182–185). Both term and preterm infants
seem to be able to form AA (20:4�-6) from linoleic acid (18:
2�-6) and DHA (22:6�-3) from �-linolenic acid (18:3�-3),
which are their respective EFA precursors (186–191) (Fig.
6); however, the degree to which the fetus is capable of fatty
acid desaturation and elongation is not clear. Although fetal
baboons have been shown to effectively synthesize both AA
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Lipid Metabolism in Pregnancy / Herrera50 Endocrine
(20:4�-6) and DHA (22:6�-3) from their respective EFA
precursors (192,193), in the newborn infant during the first
week of life, the endogenous synthesis of AA seems to con-
tribute very little to the plasma AA pool (190), the limiting
factor being a low �5 desaturation activity.
During gestation, a reduced nutritional status with respect
to EFA has been correlated to reduced neonatal growth (194),
and plasma levels of LCPUFA have been consistently corre-
lated between the mother and fetus or newborn in untreated
healthy women (195–197). After fish oil supplementation
during pregnancy, increments in DHA levels have been
found in mothers and newborns (198,199). Since these find-
ings showed the important role of dietary fatty acids during
pregnancy in controlling the supply of LCPUFA to the
fetus and newborn, supplementation with oils rich in these
fatty acids has been advised during the last trimester of preg-
nancy (198,199). However, the competitive inhibition of the
�6 and �
5 desaturases that control the conversion of EFA
into LCPUFA throughout the �-3 and �-6 pathways, caused
by an excess of specific fatty acids, may inhibit the synthe-
sis of certain LCPUFA that could be essential for fetal growth
(200). In fact, excessive intake of safflower, sunflower, or
corn oils may inhibit �6 desaturase as a consequence of their
abundance in linoleic acid (18:2�-6), inhibiting the synthe-
sis of DHA (22:6�-3) from its parent EFA precursor, �-lin-
olenic acid (18:3�-3). An excess of linoleic acid has also been
shown to decrease the formation of AA (20:4�-6) (201–205).
In addition, when fish oil was consumed, low plasma AA
levels were found (200,206). This effect was caused by the
abundance of both EPA (20:5�-3) and DHA (22:6�-3) in this
oil. These fatty acids are known to specifically inhibit �6 desat-
urase activity (207,208), although �5 and �
9 desaturase activ-
ities were also decreased in rats fed fish oil (209).
The inhibitory effects of an excess of certain dietary fatty
acids on LCPUFA synthetic pathways may acquire major
relevance during the perinatal period, where the AA has been
correlated to body weight in preterm infants (210–212).
Adverse effects of low AA concentration in blood on growth
during infancy have also been reported (210,213,214).
When polyunsaturated fatty acids (PUFA) intake is in-
creased, the PUFA content of the LDL particles increases
concordantly (215,216). The in vitro susceptibility of LDLs
to undergo oxidative modification was reported to increase
with diets rich in �-6 PUFA (215,217,218). An increase
in plasma thiobarbituric acid reactive substances (TBARs)
was also found after dietary periods of��-6 PUFA enrich-
ments (219). Whether a diet high in �-3 PUFA increases
lipid peroxidation is controversial (220,221). Whereas sev-
eral studies in humans have shown that dietary supplemen-
tation with fish oil rich in �-3 PUFA does not increase in
vivo lipid peroxidation (222–225), other studies in rats and
in cell culture have shown that this same treatment reduces
the antioxidant capacity (206,226) and enhances susceptibil-
ity to oxidative damage (227–229). Increased reactive oxy-
gen species and lipid peroxidation resulting in fetal damage,
as well as its reversion by vitamin E treatment, have been
Fig. 6. Schematic representation of desaturation and elongation of dietary essential fatty acids, as precursors of �-6 and �-3 pathways.
des., desaturase; elong., elongase; P.O., peroxisomal oxidation.
Herrera (2590).p65 12/9/2002, 8:35 AM50
Lipid Metabolism in Pregnancy / HerreraVol. 19, No. 1 51
experimentally shown to take place in diabetic pregnancy
(230–235). However, it is not yet clear whether oxidative
stress plays any role in the development of complications
in diabetic patients (236). In addition, recently, it has been
shown that treating diabetic children with high doses of
antioxidative agents, including vitamin E, has no effect on
the preservation of �-cell function or on metabolic balance
(237). In fact, as recently reviewed (238), some studies sug-
gest a potential usefulness of vitamin E in the prevention of
mutagenic effects caused by genotoxic free radicals, whereas
other studies report none.
The negative effect of high dietary fish oil intake dur-
ing pregnancy on offspring could be mediated either by the
decreased AA levels (239,240) or by an enhanced consump-
tion of �-tocopherol owing to the high LCPUFA content in
fish oil. In contrast with fish oil, dietary olive oil protects
the �-3 PUFA series (241), does not affect AA concentra-
tions (242–244), and is much more resistant to lipid peroxi-
dation (219,245,246). Thus, a comparative study of these
variables in rats fed a diet supplemented with either 10%
fish oil or olive oil as the only nonvitamin lipid during preg-
nancy and lactation was carried out (206). A decrease in both
AA and �-tocopherol concentrations as well as a delayed
postnatal development was found in the offspring of rats
fed the fish oil–rich diet (206). The study was extended to
determine whether dietary supplementation with either vita-
min E or �-linolenic acid (18:3�-6), as a precursor of AA,
could ameliorate these changes. Both AA concentrations
and postnatal development indexes, although not �-toco-
pherol concentrations, were recovered when the fish oil diet
was supplemented with �-linolenic acid. However, postnatal
development indexes were not recovered when the fish oil–
rich diet was supplemented with sufficient exogenous vita-
min E to normalize �-tocopherol levels (206). It was there-
fore concluded that low AA acid rather than �-tocopherol
was responsible for the delayed postnatal development in
the offspring of rats receiving a diet supplemented with
fish oil instead of olive oil during pregnancy and lactation.
In conclusion, since on the one hand, the safety of high
intakes of LCPUFA during pregnancy is still unclear and, on
the other, the risks and benefits of supplements with vitamin
E are not clearly determined either, additional research is indi-
cated before recommendations to increase LCPUFA intake
or to implant vitamin E treatment in pregnancy are made.
Acknowledgments
I greatly appreciate the technical help of Milagros Morante
and the editorial help of Linda Hamalainen. This work was
supported in part by grants from the Universidad San Pablo-
CEU (#10/01) and Dirección General de Investigación de la
Comunidad de Madrid (0023/00) of Spain, and by the Com-
mission of the European Communities, specific RTD pro-
gramme Quality of Life and Management of Living Resources,
QLK1-2001-00138 (PERILIP).
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